Last synced on 14 November 2025 at 11:06 pm

Laser Therapy Device

Page Type
Cleared 510(K)
510(k) Number
K202980
510(k) Type
Traditional
Applicant
Shenzhen Leaflife Technology Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/19/2020
Days to Decision
50 days
Submission Type
Summary

Laser Therapy Device

Page Type
Cleared 510(K)
510(k) Number
K202980
510(k) Type
Traditional
Applicant
Shenzhen Leaflife Technology Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/19/2020
Days to Decision
50 days
Submission Type
Summary